Steroid biochemistry.
暂无分享,去创建一个
[1] O. Hiort,et al. Understanding Differences and Disorders of Sex Development (DSD) , 2014 .
[2] N. Krone,et al. A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutism. , 2013, The Journal of clinical endocrinology and metabolism.
[3] B. Keevil,et al. The use of mass spectrometry to improve the diagnosis and the management of the HPA axis , 2013, Reviews in Endocrine and Metabolic Disorders.
[4] M. Hartmann,et al. Introduction to gas chromatography-mass spectrometry. , 2013, Methods in molecular biology.
[5] U. Steuerwald,et al. Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing , 2012, Hormone Research in Paediatrics.
[6] T. Ogata,et al. Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosterone. , 2012, Clinical chemistry.
[7] Z. Hochberg,et al. Increased activation of the alternative "backdoor" pathway in patients with 21-hydroxylase deficiency: evidence from urinary steroid hormone analysis. , 2012, The Journal of clinical endocrinology and metabolism.
[8] C. Shackleton,et al. A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency , 2011, The Journal of clinical endocrinology and metabolism.
[9] M. Dattani,et al. Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency , 2011, The Journal of clinical endocrinology and metabolism.
[10] J. Honour,et al. Recognition of 5α-reductase-2 deficiency in an adult female 46XY DSD clinic. , 2011, European journal of endocrinology.
[11] M. Hartmann,et al. Mass Spectrometry in the Diagnosis of Steroid-Related Disorders: Clinical Applications , 2011 .
[12] W. Miller,et al. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. , 2011, Endocrine reviews.
[13] G. Lavery,et al. Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS) , 2010, The Journal of Steroid Biochemistry and Molecular Biology.
[14] O. Soldin,et al. Steroid hormone analysis by tandem mass spectrometry. , 2009, Clinical chemistry.
[15] Z. Hochberg,et al. Metabolic evidence for impaired 17alpha-hydroxylase activity in a kindred bearing the E305G mutation for isolate 17,20-lyase activity. , 2008, European journal of endocrinology.
[16] C. Shackleton. Genetic Disorders of Steroid Metabolism Diagnosed by Mass Spectrometry , 2008 .
[17] U. Steuerwald,et al. Newborn screening for congenital adrenal hyperplasia: additional steroid profile using liquid chromatography-tandem mass spectrometry. , 2007, The Journal of clinical endocrinology and metabolism.
[18] N. Krone,et al. Congenital adrenal hyperplasia and P450 oxidoreductase deficiency , 2007, Clinical endocrinology.
[19] R. Auchus. The backdoor pathway to dihydrotestosterone , 2004, Trends in Endocrinology & Metabolism.
[20] C. Shackleton,et al. Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study , 2004, The Lancet.
[21] P. Stewart,et al. A Male Twin Infant with Skull Deformity and Elevated Neonatal 17–Hydroxyprogesterone: A Prismatic Case of P450 Oxidoreductase Deficiency , 2004, Endocrine research.
[22] Kenneth L. Jones,et al. The diagnosis of congenital adrenal hyperplasia in the newborn by gas chromatography/mass spectrometry analysis of random urine specimens. , 2002, The Journal of clinical endocrinology and metabolism.
[23] M. Volmer,et al. Detection of 3 beta-hydroxysteroid dehydrogenase deficiency in a newborn by means of urinary steroid analysis. , 1987, Clinica chimica acta; international journal of clinical chemistry.
[24] J. Imperato-McGinley,et al. The Diagnosis of 5α-Reductase Deficiency in Infancy , 1986 .
[25] R. E. Peterson,et al. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia. , 1985, The New England journal of medicine.
[26] A. Bongiovanni,et al. Urinary steroidal pattern of infants with congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency. , 1980, Journal of steroid biochemistry.